Posey, S. de R.L. de C.V.

FDA Device Registration & Listing · Tijuana Baja California, MX · Registration 3010699203

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3010699203
FEI Number
3010699203
Entity Name
Posey, S. de R.L. de C.V.
City/State/Country
Tijuana Baja California, MX
Establishment Address
CALLE VIA RAPIDA PONIENTE #16775 COL. NINOS HEROES ESTE, NO. 32, 33, Tijuana Baja California CP 22120, MX
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
TIDI PRODUCTS, LLC (Owner Number: 2020362)
Owner / Operator Contact Address
570 Enterprise Dr, Neenah, WI 54956, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Posey

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EAJ Apron, Leaded Radiology Class 1 892.6500 2024-10-22
NNW Bag, Urine Collection, Leg, For External Use, Non-Sterile Gastroenterology, Urology Class 1 876.5250 2012-11-18
FNL Bed, Ac-Powered Adjustable Hospital General Hospital Class 2 880.5100 2002-07-24
OYS Patient Bed With Canopy/Restraints General Hospital Class 1 880.6760 2021-12-21
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2022-12-08
KMI Monitor, Bed Patient General Hospital Class 1 880.2400 2006-05-16
PJO Fall Prevention Alarm/Sensor Combination Attached Or Unattached General Hospital Class 1 880.2400 2015-04-30
BWN Table And Attachments, Operating-Room General, Plastic Surgery Class 1 878.4950 2011-12-28
FMQ Restraint, Protective General Hospital Class 1 880.6760 2010-02-26
EYQ Garment, Protective, For Incontinence Gastroenterology, Urology Class 1 876.5920 2006-05-10
IKX Aid, Transfer Physical Medicine Class 1 890.5050 2005-04-29
FOK Pad, Neonatal Eye General Hospital Class 1 880.5270 2006-11-13
NOC Splint, Extremity, Non-Inflatable, External, Non-Sterile General, Plastic Surgery Class 1 878.3910 2011-12-28
CBH Device, Fixation, Tracheal Tube Anesthesiology Class 1 868.5770 2003-08-29
FMP Protector, Skin Pressure General Hospital Class 1 880.6450 2005-04-29
KIA Cover, Cast General Hospital Class 1 880.6185 2022-12-08
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 2005-08-17
KMK Device, Intravascular Catheter Securement General Hospital Class 1 880.5210 2005-08-17

Official Correspondent

Kelsey Weiland

US Agent Details

Amanda Altan Business: TIDI PRODUCTS, LLC Email: aaltan@tidiproducts.com Phone: (218) 5914542

Related Public Records

Same Entity

TIDI PRODUCTS, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3002563411 POSEY, S. de R.L. de C.V. TIJUANA Baja California, MX
3042176500 Posey, S. De R.L. De C.V. Tijuana Baja California, MX
3029906632 Posey S. de R.L. de C.V. Tijuana, Baja California Mexico, MX
2182318 TIDI PRODUCTS, LLC NEENAH, WI, US
3031564213 Posey, S. de R.L. de C.V. Tijuana Baja California, MX

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K935837 Healthcare Designs AIRHYTHM HEALTHCARE BED 1994-06-21
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0016-2007 Sunrise Medical CCG, Inc. 2
Joerns Ultra Care 770 Model AC Powered Beds with model numbers U770, U770 AL , U770 GNDAL. Sunrise Medical, Long Term Care Division, 5001 Joerns Drive, Stevens Point, WI 54481 USA.
Z-0017-2007 Hill-Rom, Inc. 2
Hill-Rom VersaCare Hospital Bed with optional patient pendant P3207A01 or P3207A02; model P3200.
Z-0019-2015 Arjo Hospital Equipment AB Verkstadsvagen 2
ArjoHuntleigh Contoura C1000 series beds are designed to accommodate patients weighing up to 990 lbs. (450 kg). Model C1000 is the basic bed. Model C1080 includes a weighing system and a power outlet for an ArjoHuntleigh approved mattress pump. Product Usage: The Contoura series bariatric beds are electrically operating medical beds with a maximum patient weight of 450 kg. This range is intended for use in hospitals to facilitate management of obese patients. An optional integrated weighing system helps with assessment and management of the patient if required.
Z-0026-2007 Extended Care Air Therapy Systems Inc 2
ECAT (Extended Care Air Therapy Systems) 2000 Safe Enclosure Bed

Similar Registrations

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1053541 TECHNO-AIDE, INC. Whites Creek, TN, US
2182318 TIDI PRODUCTS, LLC NEENAH, WI, US
1225473 AADCO MEDICAL, INC. RANDOLPH, VT, US
2024351 INFAB, LLC. CAMARILLO, CA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010699203. Last updated year: 2026. Please use registration number 3010699203 when referencing this establishment in official correspondence.
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